Sabrina Love Foundation
caring for kids with special needs
Mission statement:
To create a fund, which will continue in perpetuity to assist physically disabled children who require financial assistance either for equipment, medical treatment or professional help. The assistance will create in one form or another a better quality of life for these children and their families!
Our Sabrina Love Foundation was started in 2003 in memory of our daughter Sabrina. She was our darling precious child who was born with a very rare bone disorder, which effected her physical being, but not her wonderful mind. She learnt how to drive her wheelchair, even attending ballet classes all dressed in pink, and participated in all that life had to offer, with nothing but love, patience, bravery, compassion, humility and a zest that few able bodied people have. She was an inspiration to us and everyone who met her and we were the lucky parents blessed to have her share our lives for six years, a month short of her seventh birthday.
caring for kids with special needs
caring for kids with special needs
Mission statement:
To create a fund, which will continue in perpetuity to assist physically disabled children who require financial assistance either for equipment, medical treatment or professional help. The assistance will create in one form or another a better quality of life for these children and their families!
Our Sabrina Love Foundation was started in 2003 in memory of our daughter Sabrina. She was our darling precious child who was born with a very rare bone disorder, which effected her physical being, but not her wonderful mind. She learnt how to drive her wheelchair, even attending ballet classes all dressed in pink, and participated in all that life had to offer, with nothing but love, patience, bravery, compassion, humility and a zest that few able bodied people have. She was an inspiration to us and everyone who met her and we were the lucky parents blessed to have her share our lives for six years, a month short of her seventh birthday.
caring for kids with special needs
caring for kids with special needs
OBJECTIVE 1: To Assist Physically disabled children from disadvantaged communities in Bitou to access the special care,medicalattention,treatment,equipment, proffessional services they require to reach their full potential.
OBJECTIVE 2: To assist physically disabled children in Bitou to access the special education they need to achieve their full potential(intellectual,physical,social and emotional)
OBJECTIVE 3: To empower parents to overcome/cope with the challenges of raising a special needs child and build capacity within SLF
OBJECTIVE 4: To promote acceptance and integration of disabled children and their families into society by raising awareness of how community members can assist them to overcome their challenges
OBJECTIVE 5: To create & maintain a fund,which will continue in perpetuity to assist disabled children in Bitou who require financial assist to access what they need to reaqch their full potential
OBJECTIVE 6: To provide support to severely intellectually disabled children & their families in the Bitou area by establishing a partnership with Die Sterreweg DC centre
caring for kids with special needs
caring for kids with special needs
Through the Sabrina Love Foundation we are able to help and hopefully reach so many of these special little people and their families in and around Plettenberg Bay, and teach others what a difference it can make.
Elethu
Robin Windvogel
Birth date: November 29 2007
Lives in: Green Valley
Schooling at: Wittedrift Primary School
Challenges this child faces: Robin has a skin condition which causes her skin to thicken and break out in sores. It gives her a lot of pain. She also has arthritis which makes it very difficult for her to move around or be bumped or touched by other children.
Personal story: Robin is living in Green valley with her mother Luzaan and older brother Fabian. She started getting the skin condition when she was still very small but then it changed and became more severe and arthritis started as well. She is a sweet and sad child because she cannot play with other children very much because of her difficulty in moving and her fear of being bumped or touched. We want so badly to see Robin running and playing with the children in her street.
She has been on very strong medication throughout her life but the doctors have not been able to exactly diagnose her condition. Dr Rachel Bouwer of Plett has now given her a homeopathic cream which seems to be helping.
Inathi Sobayeni
Birthdate: 20 April 2009
Lives in: Kwanokuthula
Challenges this child faces: Inathi has to attend Red Cross Hosptial every month and is often going to knysna hospital, as he gets sick very often. He is currently receiving weekly Occupational Therapy to assist with his developmental delay. Inathi recently had his tracheostomy removed, making caring for him much easier.
Personal story: Inathi was born on the 20th of April 2009 with no complications or childhood illness but at 3 months he developed a lung disease and at 6 months had to have a tracheostomy to assist with breathing. His mom has to stay at home with him to change the tracheostomy and look after him .He is so loved by both his parents, who are determined to do whatever they can to keep him healthy and help him progress both medically and developmentally. Inathi’s smile really does light up the room!
Evan Kamer
Birthdate: December 28 2009
Lives in: New Horizons
Challenges this child faces: He has had so many challenges, including one lung being bigger than the other, his kidneys are not functioning properly and had to have a vesicostomy, which is a surgically-created connection between the urinary bladder and the skin which is used to drain urine from the bladder. Despite all these physical setbacks, Evan is very loved and captures the hearts of everyone he meets.
Personal story: Evan was born on the 28th of December 2009. He has been diagnosed with spina bifida but more specifically split cord malformation, meaning that he had a bony protrusion into his spinal cord, which had to be surgically removed. He has had a tough time since he was born and has spent most of the first few months of his little life in hospital.
Max Hofmeyer
Lives in: Plettenberg Bay
Schooling at: Plett Pre Primary
Challenges this child faces: Max is a 6 year old little boy who was diagnosed mild autism when he was younger. He recently also developed juvenile arthritis and has become one of the Sabrina love foundation children..
Personal story: Max was recently accepted into a special school in George, and although his mom will be sad not to be with him every day, she knows he will shine.
Siyamthanda Mdzeke
Siyamthanda was born on the 1st of December 2005, she is staying in Kwanokuthula. She developed a problem with walking when she was 10 months old her toes began to bend.
She had an operation to fix her feet and she gets regular exercise assessments with an OT (Nicole).
Siyamthanda will be doing her Grade R in Phakamisani Primary next year.
Aidon De Lange
Aidon was born on the 10th of July 2000; he is staying in New Horizons. He was born with a hole in his heart.
He has been operated on and it is partially fixed. He is not gaining weight; he is also often blue around his eyes and mouth. Aidon attends school at Formossa Primary.
Jadi Mondeka
Jadi was born on the 3rd of May 2006, she is staying in Kranshoek. She is partially deaf, she was given a hearing aid but she throws it away. When she was one year old, her mother noticed that she was very quite as a baby and that she couldn’t hear.
She has never learned to talk. The doctors said that she needs to use the hearing aids and maybe she will be able to hear one day.
Jadi is going to attend school in De la Bat School for the Deaf next year.
Creshne’ Terblanche
Birthdate: 19 May 2010
Challenges this child faces: She is slightly behind in her development, and receives weekly OT to help her catch up.
Personal story: Creshne’ is a 9 month old little girl who had a shunt put in when she was 1 month old, because she has hydrocephalus as well as a cyst on her brain.
Glenville Paulsen
Glenville was born on the 8th of December 2001, he is staying in Crags. He have a congenital heart defect, he recently went to Red Cross for the operation and will be going for check-ups. Glenville goes to school at The Crags Primary School.
Glenville is also receiving Epap which will assist him for nutrition as he is skinny.
Elton October
Birthdate: June 8 2000
Lives in: Kranshoek
Schooling at: Kranshoek Primary
Challenges this child faces: Elton was born with one leg shorter than the other. Because of not receiving any attention for it he has always walked on tip toe and now his aquilles tendon has shortened. It will require surgery to repair it.
Personal story: Elton’s mother left him with his grandparents when he was a baby and they now care for him. They are extremely poor and need help. He is friendly and enthusiastic about things and is very excited to be one of the Sabrina family.
Chouwaine Le Port
Birthdate: 27 March 2005
Lives in: Kranshoek
Challenges this child faces: Chouwaine’s mom finds it difficult to buy clothes for him and he is unable to wear any shoes. After numerous investigations, it has been decided to amputate his foot in 2011.
Personal story: Chouwaine has a diagnosis of Proteus Syndrome, which has resulting in him having one leg and foot larger than the other. He lives with his mom and dad in Kranshoek. He will be starting preschool in 2011.
Lemischa Andrews
Birthdate: 7 February 2005
Lives in: Wittedrift
Schooling at: Mainstream preschool
Challenges this child faces: Lemischa is finding it very difficult to cope with the mainstream school system. She will be attending Carpe Diem, a special school in George in 2011.
Personal story: Lemischa has a diagnosis of mild Cerebral Palsy, right hemiplegia. She lives with her mom and dad in Wittedrift and has been attending a mainstream Preschool. She is a very friendly, bubbly little girl.
Percy Van Rooyen
Birthdate: 10 December 1993
Lives in: New Horizons
Schooling at: Squid-protective workshop
Challenges this child faces: Miller-Dicker symdrome is quite a rare disorder. He has had numerous operations and is unable to walk, relying on either his powered or manual wheelchair to get around. He recently had a ramp put in outside his house so that his mother does not need to pick him up every time he wants to go outside.
Personal story: Percy was diagnosed with Miller-Dicker Syndrome when he was young. He lives with his mom and dad in New horizons and works at a protective workshop in Plett called Squid. He is a very positive young man, who is at every single Sabrina Love Foundation event.
Lesley Ann Martins
Lives in: Kranshoek
Challenges this child faces: Lesley Ann has to go for regular checkups to George and Red Cross Hospital
Personal story: Lesley Ann has a congenital heart conditions. She lives with her school going mom and grandmother in Kranshoek.
Chaldrin Julies
Birthdate: 18 November 2003
Lives in: Kranshoek
Schooling at: Mainstream schooling
Challenges this child faces: Chaldrin is a very shy little boy and does not socialise very easily. It has been very difficult to assess his actual vision and this makes it difficult to refer him to the correct school. His mom does not want him to go all the way to Cape Town and there are no other schools for visually impaired children close by. He will be attending a mainstream grade R class with an assistant in 2011.
Personal story: Chaldrin has a severe squint and partial blindness. He had cataracts removed in 2006, but is still unable to see well. He lives with his mom and dad in Kranshoek.
Jayline Ockhuis
Birthdate: 31 May 2007
Lives in: The Crags
Challenges this child faces: Jayline’s foot was operated on when she was little but her foot has not maintained the corrected position. She is due for another operation in 2011
Personal story: Jayline was born with a club foot and lives with her mom and grandmother in the Crags.
Zinedene Delport
Birthdate: March 10 2005
Lives in: New Horizons
Schooling at: Sterreweg Day Care Centre
Challenges this child faces: Zinnie’s mother Mary contracted the CMV virus when he was in utero and it affected his heart. He requires major heart surgery. His development was also affected in other areas.
Personal story: Zinnie lives with his mom and dad, Mary and Nathan, and his brother Breyton. He goes to the Sterreweg day care centre in the day and Mary goes with him because he needs constant monitoring until he has heart surgery. Zinnie contracted the CMV virus in utero and as a result he was born with a heart defect. He fought bravely for survival and has travelled twice to Red Cross Hospital in Cape Town with his parents, expecting major heart surgery to be performed only to get there and find out that the time was not quite right. He needs to put on weight before surgery can be performed so now he is on a protein powder supplement. Sabrina Love Foundation is supporting his mother, Mary, so that she can stay at home with him and help him to gain weight and get stronger. We also pay for his transport when he is taken to hospital or rushed to the emergency room.
Lusanda Lawrence
Lusanda was born on the 14th of August 1999; she is staying with her aunt in Pine trees. She is deaf, the Foundation has assisted her through studying at De la Bat School for the deaf.
Her mother is deceased and her father who is in Uitenhage in Eastern Cape doesn’t take care of Lusanda that is for the reason that Lusanda came to Plettenberg bay to stay with her aunt.
Jone’ Booysen
Birthdate: 18 June 2009
Challenges this child faces: She is waiting for a much needed operation to remove the cataract from her eye.
Personal story: Jone’ was born 4 months premature and is slightly blind in one eye.
Xolisa Dinga
Birthdate: 29 June 1994
Lives in: Kwanokuthula
Schooling at: Murray High School
Challenges this child faces: Both his feet were amputated after he contracted a disease in 2004.
Personal story: Xolisa’s mother passed away in 2003. Shortly after that he contracted an illness which resulted in infections in his feet and partial amputations of both feet. He lives with his grandmother. When we met him we arranged for him to get special ‘shoes’ so he could walk and for a short while this worked but then his Achilles tendon contracted and it caused a lot of pain. He went onto crutches and then a wheelchair. At the beginning of 2008 he had surgery to amputate the rest of one foot and most of the other so that he could be fitted with proper prosthetics. Mike barkley and his team in George did a fabulous job and soon he was back in Plett walking around. However getting to school was a slow process so we bought him a bicycle and now he’s the fastest on the block.
Xolisa is a great soccer lover and coaches a team.
Christiano Lutters
Birthdate: August 25 2007
Lives in: Kranshoek
Challenges this child faces: Christiano had to have a shunt put in his brain soon after he was born. He also had to have a tracheostomy so that he can breathe properly. He has a condition which does not allow him to open his mouth wide enough and this has at times impaired his breathing.
Personal story: Christiano was born to a school going mother Segourney, who was hoping to return to school. However the difficulties that this little fellow has faced in the early part of his life have prevented her from returning to school and she takes care of him herself full time. He is scheduled to have surgery to fix his jaw and His grandmother also takes care of him a lot and he is a very spirited and lively baby. In fact he is a big handful for his mother who has to watch him very carefully because he is not allowed to bump his head due to the shunt that has been put there.
Marlon Marcus
Birthdate: March 14 2001
Lives in: New Horizons
Schooling at: Formosa Primary in New Horizons, Plettenberg Bay
Challenges this child faces: Marlon was born with no fingers on his right hand.
Personal story: Marlon lives with his parents and older brother and younger sister. He is kind and friendly. He manages amazingly well with his one hand but is self conscious of the other one. When Mike Barkley met him he explained to him that it was possible to have surgery to attaché prosthetic fingers to, but marlin really didn’t want to have an operation so they made a sort of sleeve for him and by putting pressure against it he can grip things.
Cecil Winston Majavie
Birthdate: September 3 1992
Lives in: Kranshoek
Schooling at: Kranshoek Primary in Plettenberg Bay
Challenges this child faces: Cecil was born with one arm and one leg shorter than the other.
Personal story: Cecil is a delightful and smart child. He lives with his mother and helps her around the house a lot. He is active and playful. He has been receiving physio from Colleen Kemp and Mike Barkely fitted him with special braces for his feet to keep his spine straight while walking so that his spine doesn’t become deformed.
Oliver Heers
Birthdate: February 18 1993
Lives in:New Horizons
Schooling at: Carpe Diem in George
Challenges this child faces: Oliver developed TB meningitis when he was 2yrs old. He became paralysed on the left side of his body and also suffered from cognitive impairment.
Personal story: After undergoing an operation Oliver is able to walk and use the left side of his body better, however he is still somewhat physically impaired and has a concentration problem and cognitive challenges.
Oliver lives with his parents in New Horizons in Plettenberg Bay. He is a very warm and friendly child.
Sabrina Love Foundation helps him and his family by paying for his school fees, uniform and transport to Carpe Diem School in George, which is a school for special needs children.
caring for kids with special needs
caring for kids with special needs
Ruwan Barnard
Birthdate: June 30 2008
Lives in: Kranshoek
Challenges this child faces: Ruwan was born with three holes in his heart. One has been surgically closed but there are still two which will be closed when he is a little older.
Personal story: Ruwan’s mom Natashe works as a cleaner for the municipality. His aunt looks after him while she is at work.
Amy Cloete
Birthdate: November 20 1995
Lives in: Kranshoek
Schooling at: Amy has attended Plettenberg bay Primary School and graduated from there. She will be going to Wittedrift High School in 2009.
Challenges this child faces: Amy was born with a syndrome that causes one side of her body to be larger than the other.
Personal story: Amy is a quiet and very respectful child. She lives with her family in Kranshoek and loves playing with her friends , reading or playing sports. She is the daughter of Mary Cloete who helps Ayesha and Shani.
Wanda Mhlambiso
Birthdate: July 26 1997
Lives in: Qolweni
Schooling at: Athlone School for the Blind
Challenges this child faces: Wanda is blind and due to an operation to remove a tumour he now has a shunt in his brain for draining fluids. He needs to attend a special school for the blind and he also needs to take medication to control his passing of water.
Personal story: Wanda is a very spirited and friendly child with a sense of humour and joy in life. He was going to the Squid daycare program when he was brought to our attention and the workers there were fundraising to try and get him back into school. He had been attending the Athlone School for the Blind but when his mother, Bukeka, moved to Plettenberg Bay he was no longer able to attend. He has a brother of 5 and a baby sister.
Racquelle McCallum
Birthdate: 12 June 1995
Lives in: New Horizons
School: Kelly attends Formosa Primary School.
Challenges: Takayasu’s Disease, which causes blood clots and blood vessel aneurisms. She lost one kidney due to bloodclots. She has to be on immunosuppressive medication all the time.
Personal story: Kelly loves playing with her friend and cousins. Her family is also very very important to her
Shani Catherine Martins
Birthdate: 21 Nov 1993
Lives in: Kranshoek
School: Shani goes to Kranshoek Primary but she get privately tutored there as she does not fit in with any of the classes.
Challenges: Shani was born with Spina Bifida and is a paraplegic.
Personal story: Shani gets picked up every morning by Auntie Mary who is like a second mother to her. She then goes to school where Ms Wilhelmina Lumka tutors her and then she returns to Mary’s house in the afternoons until her mother Dora returns from work. She was quite old before she started getting specialised attention and so many of her learning pathways had already closed so she is very far back in her scholastic learning. However she would like to work as a clerk one day and often watches Mary’s daughter Marlene in her administrative position.
Vuyolwethu Mbala
Birthdate: 19 Nov 1992
Lives in: Qolweni
School: Vosh goes to Carpe Diem in George for children with special needs.
Challenges: Vosh has a mild cerebral palsy.
Personal story: Vuyolwethu (Vuyo) Mbala is attending Carpe Diem School in Georgeand lives in the informal settlement of Qolweni. She is is such a delightful person and well liked by all her classmates.
Luche McCullum
Birthdate: 27 Feb 1993
Lives in: New Horizons
School: She goes to school at Plett Sekonder.
Challenges: Luche had kidney failure and a close encounter with death. She was very very sick and then had one kidney removed. She is doing quite well now but is still on medication to slow down any further kidney failure.
Personal story: Luche lives with her grandmother in New Horizons. She is very active in her church, and spends quite a lot of her time in her church youth group.
Darryn Tekane
Birthdate: 21 Sept 1992
Lives in: New Horizons
School: Darryn attends Carpe Diem School in George
Challenges: Darryn has a spinal condition which inhibits his growth. He is as tall as a normal 3yr old.
Personal story: Darryn is one of three siblings in a single parent family. His father Daniel takes care of his younger brother and sister as well as him. He is a brave and resilient young man in a very small body with a deep voice.
Beauty Nomhle Tyam
Birthdate: March 13, 1997
Lives in: Kwanokuthula
School: Beauty attends the de La bat School for the Deaf in Wocester.
Challenges Beauty faces: Beauty is deaf.
Personal story: Beauty Tyam lives with her family in Kwanokhuthula when she is not at school. She stays at the hostel in Worcester during school times where she has many friends and is liked by everyone. She has brothers and sisters in Kwanokuthula. This year we made it possible for her mother to can stay with her at Beauty’s school so that she was able to learn some sign language so that they can communicate better.
Ayesha Majavie
Birthdate: July 9 2003
Lives in: Kranshoek
Schooling at: Pinelands
Challenges Ayesha faces: Ayesha was born with Spina Bifida. She is unable to walk on her own and needs either a wheelchair or crutches. She is getting regular help from an occupational therapist and physiotherapist who are helping her learn to walk with splints and crutches. She makes regular trips to Red Cross Hospital in Cape Town.
Personal story: Ayesha is a bright affectionate child living with her parents Denise and Charles and her two older sisters, Danielle and Shane in Kranshoek. They are devoted to her and are helping her learn to do things. She has been a Sabrina Love Foundation child since she was 3 and for awhile attended the Sterreweg Day Care Centre where she had a chance to interact with lots of other children who face challenges. Everyone loves her. She now attends a regular preschool and is preparing to enter the mainstream Primary School in Kranshoek. She has a carer, Shirley, who goes to the preschool several times a day to take care of her bathroom needs.
caring for kids with special needs
caring for kids with special needs
Help us to create a fund, which will continue in perpetuity to assist physically disabled children who require financial assistance either for equipment, medical treatment or professional help. The assistance will create in one form or another a better quality of life for these children and their families!
Wishlist
Physiotherapist Speech – Care Givers:
We have a full time qualified Occupational Therapist, Nicole McDonald, who works one on one with over 25 of our children.Therapy ranges from child to child as each child is different and unique and so are their needs. One of her biggestchallenges is trying to fulfil the role of a speech and physiotherapist as well. Our children are currently going to George forSpeech Therapy. We would love to be able to afford an inhouse Speech Therapist and Physiotherapist to ensure ourchildren receive the best therapy we can offer.We have a full time qualified Occupational Therapist, Nicole McDonald, who works one on one with over 25 of our children.Therapy ranges from child to child as each child is different and unique and so are their needs. One of her biggestchallenges is trying to fulfil the role of a speech and physiotherapist as well. Our children are currently going to George forSpeech Therapy. We would love to be able to afford an inhouse Speech Therapist and Physiotherapist to ensure ourchildren receive the best therapy we can offer.
Hospital Bills / Transport Costs – Medical Assistance:
We have 47 Sabrina Love children and 25 Sterreweg children, allneeding medical care. We aim to assist them not only with costsinvolved in the medical care of these children, but also in gettingthem to and from each and every appointment. Some children need to go as far as Cape Town, Red Cross Hospital formedical procedures. The cost of transporting the children and caregivers is on going and a constant challenge.Hospital Bills Medical AssistanceWe have 47 Sabrina Love children and 25 Sterreweg children, allneeding medical care. We aim to assist them not only with costsinvolved in the medical care of these children, but also in gettingthem to and from each and every appointment. Some children need to go as far as Cape Town, Red Cross Hospital formedical procedures. The cost of transporting the children and caregivers is on going and a constant challenge.
Stipends – Family Bonds
Nothing is more important to Sabrina Love Foundation than the bonds formed in a family unit. We strive to equip andempower our families to cope with the everyday challenges of raising a disabled child, as a family unit. We assist parentsfinancially by providing a small stipend each month so that the main guardian or parent is able to remain at home, caring fortheir children. No one knows a child better than their own parent. We pride ourselves in being able to help nurture and protectthe family bonds.Nothing is more important to Sabrina Love Foundation than the bonds formed in a family unit. We strive to equip andempower our families to cope with the everyday challenges of raising a disabled child, as a family unit. We assist parentsfinancially by providing a small stipend each month so that the main guardian or parent is able to remain at home, caring fortheir children. No one knows a child better than their own parent. We pride ourselves in being able to help nurture and protectthe family bonds.
Banking details
Sabrina Love Foundation
First National Bank
Account # 62053720556
Branch code 210514 (Plettenberg Bay)
caring for kids with special needs
caring for kids with special needs
March 9, 2013
The Grand Café : Pre-Argus dinner and fun with ‘Sabrina’
Join our Sabrina Love Cycle Team as we prepare for the Cape Argus Pick n Pay Cycle Tour the evening before our BIG DAY. Book to join the Sabrina Love Pre Argus Dinner Feast at The Grand Cafe Beach, Waterfront, Cape Town on Saturday March 9, 2013, arrival from 18h00 through 21h00. R150 per person.
This will be a great time to get to meet our fellow cyclists and share more of our Sabrina journey.
Limited seating so please book early. Family members welcome to join and book.
March 10, 2013
Cape Argus Pick n Pay Cycle Tour 2013
ENTRIES ARE CLOSED
Entries are closed but you can upgrade to a group early start > GO HERE
Ride with the Sabrina Love Team and you will be guaranteed an early start, super cool goody bag, special area for race pack collection and most importantly, you help change a child’s world.
By Joining the Sabrina Team, the ‘package’ includes:
- Guaranteed entry.
- Earlier start time. Guaranteed to start before PPA and open riders. (Before 16000 riders!) Sabrina riders who qualify for an even earlier start will still be seeded accordingly with the option to drop down to ride with their colleagues.
- Special ‘goody bag’.
- Special area at registration for collection of race packs.
- Your contribution to The Sabrina Love Foundation – Caring for children with special needs.
Last years team was 260 riders, this year we are aiming for 400! The aim is to raise much needed funding for the Foundation and also to have a wonderful experience with friends and newly made acquaintances. The riders entering in the group has grown substantially and has become a great social event too. Riders will participate with the same group year on year and it has become a great re-union and offers time out for people to compare notes and catch up with each other.
Although it cost a little more to ride with our Charity, you can be rest assured that, although the Cape Argus Pick n Pay Cycle Tour claim the full charity fee, the small profit made goes directly to our children. And 100% of profits made from the cycle shirt goes to change a childs world.
JOIN THE SABRINA LOVE ARGUS 2013 TEAM, ride in pink, and help change a life.
caring for kids with special needs
caring for kids with special needs
Physical Address: No Street Address
Postal Address: PO Box 1741
Plettenberg Bay
Postal Code: 6600
Telephone: +27(0)445333130
Mobile: +27(0)720634443
Email: stars@sabrinalove.co.za
Directions: -
Latitude: -34.056855
Longitude: 23.371954